胆酸端部树突状赖氨酸-聚乙二醇-块状树突状赖氨酸的合成及其对紫杉醇水溶性的增强作用

KIMIKA Pub Date : 2018-12-27 DOI:10.26534/KIMIKA.V29I2.36-43
Laurenzo D V Alba, Mario Enriquez
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引用次数: 0

摘要

紫杉醇是一种用于抑制癌细胞有丝分裂的化疗药物,由于其水溶性较差,需要使用增溶剂Cremophor EL。然而,Cremophor EL与化疗后的不良反应有关。本文报道了一种紫杉醇替代增溶剂的合成。通过二环己基碳二酰亚胺(DCC)介导的缩合反应,将两代树状赖氨酸偶联到PEG-4000的两端,并用30%的哌啶脱保护。通过DCC/n-羟基琥珀酰亚胺将胆酸连接到末端氨基上。采用电喷雾电离质谱法对合成步骤进行了监测和验证。结果表明,所合成的聚合物是一种可行的紫杉醇输送增溶剂。需要进一步的研究来评估其安全性和稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of cholic acid-terminated dendritic lysine-block-poly(ethylene glycol)-block-dendritic lysine and its enhanced ability to solubilize Paclitaxel in water
Paclitaxel, a chemotherapeutic drug used to inhibit mitosis in cancer cells, requires the use of the solubilizer Cremophor EL due to its poor water solubility. However, Cremophor EL is associated with adverse reactions following chemotherapy. This work reports the synthesis of an alternative solubilizing agent for paclitaxel. Two generations of dendritic lysine were coupled onto both ends of PEG-4000 via reaction of fluorenylmethyloxycarbonyl (FMOC)-lysine-FMOC-OH with dicyclohexylcarbodiimide (DCC)-mediated condensation, and deprotection with 30% piperidine. Cholic acid was attached to the terminal amino groups through the use of DCC/n-hydroxysuccinimide. Synthesis steps were monitored and confirmed by electrospray ionization mass spectroscopy. The results suggest that the synthesized polymer is a viable solubilizing agent for delivery of paclitaxel. Additional studies are required to assess its safety and stability.
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